126759-30-6 Usage
Description
Methyl 3-bromo-4-nitrobenzoate is a chemical compound derived from benzoic acid, featuring a methyl group, a bromine atom, and a nitro group attached to a benzene ring. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals and serves as a building block for complex organic molecules. This yellow crystalline solid is typically handled with care due to its potential irritant and toxic properties.
Uses
Used in Pharmaceutical Industry:
Methyl 3-bromo-4-nitrobenzoate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
Methyl 3-bromo-4-nitrobenzoate is used as an intermediate in the production of agrochemicals, playing a crucial role in the creation of compounds that can enhance crop protection and yield.
Used in Organic Synthesis:
Methyl 3-bromo-4-nitrobenzoate is used as a building block in organic synthesis for its potential to form complex organic molecules, contributing to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 126759-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126759-30:
(8*1)+(7*2)+(6*6)+(5*7)+(4*5)+(3*9)+(2*3)+(1*0)=146
146 % 10 = 6
So 126759-30-6 is a valid CAS Registry Number.
126759-30-6Relevant articles and documents
Synthesis of phenazine-2,8-dicarboxylates
Bhadbhade, Mohan M.,Constable, Grace E. O.,Hunter, Luke,Jung, Jane,Read, Roger W.,Wakelin, Laurence P. G.
supporting information, (2022/01/12)
Phenazine is a tricyclic heteroarene that forms the core of diverse functional molecules including DNA intercalators. However, 2,8-disubstituted phenazines are rare, and this potentially limits the medicinal development of this class of heterocycles. Here we describe the synthesis of two new members of this compound class (i.e. dimethyl phenazine-2,8-dicarboxylate and the corresponding diacid), following a synthetic route that involved inter- and intramolecular Buchwald-Hartwig N-arylations. We also detail a simple NMR-based method for proving the 2,8-disubstitution pattern, in order to counterbalance suspected structural misassignments elsewhere in the peer-reviewed and patent literature.
